2-Chlorotoluene → Mepronil

HRID 847439

반응식

HRID 847439 반응식
Cl[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH3:8].[CH:9]([O:12][C:13]1[CH:14]=[C:15]([CH:17]=[CH:18][CH:19]=1)[NH2:16])([CH3:11])[CH3:10].C1(P(C2C=CC=CC=2)CCCCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C:50](=[O:53])([O-])[O-].[Na+].[Na+].[C]=O>[Pd](Cl)Cl>[CH:9]([O:12][C:13]1[CH:14]=[C:15]([CH:17]=[CH:18][CH:19]=1)[NH:16][C:50]([C:2]1[C:3]([CH3:8])=[CH:4][CH:5]=[CH:6][CH:7]=1)=[O:53])([CH3:11])[CH3:10]

참가 물질

7

실험 절차

In an autoclave made of a metal were placed 12.7 g of ortho-chlorotoluene, 3 g of meta-isopropoxyaniline, 17.7 mg of palladium chloride, 426 mg of 1,4-bisdiphenylphosphinobutane and 23 g of sodium carbonate. The air in the autoclave was replaced with carbon monoxide introduced thereinto in several times, after which carbon monoxide was further introduced to adjust its pressure therein to 30 kg/cm2. The internal temperature was adjusted to 200° C. on a salt bath and the reaction was carried out thereon with stirring for 5 hours. After completion of the reaction, the reaction mixture was cooled to room temperature and washed with water. Subsequently, the organic layer was separated, concentrated, and then recrystallized from ethyl acetate-hexane to obtain 2.6 g of 3'-isopropoxy-2-toluanilide.

후처리

  1. additionintroduced
  2. customThe internal temperature was adjusted to 200° C. on a salt bath
  3. customAfter completion of the reaction
  4. washwashed with water
  5. customSubsequently, the organic layer was separated
  6. concentrationconcentrated
  7. customrecrystallized from ethyl acetate-hexane

출처 및 근거

ORD 기록
ord-81bb1e42211c462193f358be22cb9a7e
출처 데이터셋
uspto-grants-1992_08
특허 번호
US05142057

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